First-order isotropic–smectic-A transition in liquid-crystal–aerosil gels

M. K. Ramazanoglu, P. S. Clegg, R. J. Birgeneau, C. W. Garland, M. E. Neubert, and J. M. Kim
Phys. Rev. E 69, 061706 – Published 4 June 2004

Abstract

The short-range order which remains when the isotropic to smectic-A transition is perturbed by a gel of silica nanoparticles (aerosils) has been studied using high-resolution synchrotron x-ray diffraction. The gels have been created in situ in decylcyanobiphenyl, which has a strongly first-order isotropic to smectic-A transition. The effects are determined by detailed analysis of the temperature and gel density dependence of the smectic structure factor. In previous studies of the continuous nematic to smectic-A transition in a variety of thermotropic liquid crystals the aerosil gel appeared to pin, at random, the phase of the smectic density modulation. For the isotropic to smectic-A transition the same gel perturbation yields different results. The smectic correlation length decreases more slowly with increasing random-field variance in good quantitative agreement with the effect of a random pinning field at a transition from a uniform phase directly to a phase with one-dimensional translational order. We thus compare the influence of random fields on a freezing transition with and without an intervening orientationally ordered phase.

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  • Received 27 November 2003

DOI:https://doi.org/10.1103/PhysRevE.69.061706

©2004 American Physical Society

Authors & Affiliations

M. K. Ramazanoglu, P. S. Clegg*, and R. J. Birgeneau

  • Department of Physics, University of Toronto, Toronto, Ontario, Canada M5S 1A7

C. W. Garland

  • Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA

M. E. Neubert and J. M. Kim

  • Liquid Crystal Institute, Kent State University, Kent, Ohio 44242, USA

  • *Present address: School of Physics, University of Edinburgh, Mayfield Road, Edinburgh EH9 3JZ, U.K.

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Vol. 69, Iss. 6 — June 2004

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